QA Officer Document Control

QA Officer Document Control – 6-month contract or permanent position – Netherlands

Our client is a fast growing, biopharmaceutical contract development and manufacturing organization (CDMO) focused on viral vector and recombinant protein products. They have recently built a state-of-the-art GMP manufacturing facility at the Bio Science Park in Leiden that is getting filled with exciting new vaccines, antibodies and protein products. They support customers with the development & commercialization of biologics enabling the treatment & prevention of life-threatening conditions such as cancer, COVID-19, influenza and other infectious diseases.

Currently they are working on the production of a leading COVID-19 vaccine. If you too would like to contribute to this challenging and fulfilling activity and become part of an inspiring biotech services company, then this is a perfect opportunity for you!

Key Responsibilities:

• As the QA Officer Document Control you are responsible for the Development, Maintenance, Coordination, Execution and Continuous Improvement of the GxP, Documentation System.
• The QA Officer Document Control will be responsible for the coordination of new and changes for revision of existing controlled documents, including masters and templates.
• You will manage the issuance, reconciliation and retrieval of the GxP documentation such as Batch Records, Component Records and Logbooks.
• You will ensure compliance with GMP Regulatory Requirements, Policies and Procedures

 
Key Requirements:

• As the QA Officer Document Control you will have a minimum of 3 years’ experience of working in a similar role within the Pharmaceutical industry.
• The QA Officer Document Control will have strong knowledge of GMP requirements.
• As the QA Officer Document Control experience with Lean Management and 6 Sigma Methodology with be highly advantageous.

If you feel that this opportunity is for you and you match these requirements, then please apply now.




The candidate must have the rights to work in the location stated in the job advert.

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